Tetraphenylbenzosilole: An AIE Building Block for Deep-Blue Emitters with High Performance in Nondoped Spin-Coating OLEDs.

1,1,2,3,4,5-Hexaphenylsilole (HPS) is a star building block of aggregation-induced emission luminogens (AIEgens) in constructing OLED emitters. However, their development is obstructed by their complicated preparation and difficulty of achieving blue/deep-blue emission via structure modification and tuning. In this study, a benzo-group modification strategy was adopted to increase the skeleton rigidity and reduce the vibrational-rotational motion of peripheral substituted phenyl groups.

Selective Cu(ii) sensing by a versatile AIE cyanostilbene-based gel system.

Cyanostilbene-based derivatives 1-3 were designed, synthesized and fully characterized. By screening their gelating abilities, we observed that the subtle difference in the position of the pyridine nitrogen greatly affected the resulting fluorescence and gelation properties. Notably, 1 was found to be a versatile ambidextrous gelator capable of forming organo-, hydro-, and Cu(ii) specific metallogels.

Self-Complementary Dimers of Oxalamide-Functionalized Resorcinarene Tetrabenzoxazines.

Self-complementarity is a useful concept in supramolecular chemistry, molecular biology and polymeric systems. Two resorcinarene tetrabenzoxazines decorated with four oxalamide groups were synthesized and characterized. The oxalamide groups possessed self-complementary hydrogen bonding sites between the carbonyls and amide groups.

Magnetostructural Characterization of Oxalamide Dihalo-Bridged Copper Dimers: Intra- and Interdimer Interactions Studied by Single-Crystal Electron Spin Resonance Spectroscopy.

Detailed single-crystal electron spin resonance (ESR) analysis of oxalamide complexes with halogen-bridged copper dimers, supported by X-ray, magnetic susceptibility, and powder ESR studies, is reported. Four complexes with two different ligands are synthesized: [CuL (μ-X)] and [CuL (μ-X)] , for which L =N-(l-alanine methyl ester)-N'-[(2-pyridine-2-yl)methyl]oxalamide and L =N-(l-valine methyl ester)-N'-[(2-pyridine-2-yl)methyl]oxalamide, for which X=Cl or Br. X-ray analysis shows that the geometry at each copper(II) ion is square pyramidal, whereas two pyramids share one base-to-apex edge with parallel basal planes.

Cu(II)-specific metallogel formation by an amido-anthraquinone-pyridyloxalamide ligand in DMSO-water.

This study on the CuCl2-induced and water-mediated metallogel formation by a pyridine containing anthraquinone-based ligand in DMSO provides significant insights on the relationship between the coordination geometry and metallo-gelation aptitude for a series of variably substituted pyridyloxalamide ligands.

Crystal structures and magnetic properties of a set of dihalo-bridged oxalamidato copper(II) dimers.

A set of four copper(ii) complexes, and (X = Cl, Br; = N-(l-leucine methyl ester)-N'-((2-pyridin-2-yl)methyl)oxalamide and = N-benzyl-N'-((2-pyridin-2-yl)methyl)oxalamide), have been synthesized and characterized by X-ray structural analysis, electron paramagnetic resonance (EPR) spectroscopy on single crystals and by SQUID magnetization measurements. X-ray diffraction studies show one-dimensional hydrogen bonded networks of dimeric copper(ii)-complexes bridged by two halide ions and with the two metal centers 3.44-3.

New frontiers in hybrid materials: noble metal nanoparticles--supramolecular gel systems.

The last decade has witnessed an increasing interest in the development of hybrid materials with novel properties. Noble metal NPs-gel materials represent a new class of hybrid composites, envisaged by many to have great potential for technological applications, as a consequence of the beneficial integration of the properties of both the NPs and the gelling compounds. This review article provides an up-to-date account of the most interesting and inspiring works published in the field, especially focusing on their preparation and characterization.

Preparation of potentially porous, chiral organometallic materials through spontaneous resolution of pincer palladium conformers.

Understanding the mechanism by which advanced materials assemble is essential for the design of new materials with desired properties. Here, we report a method to form chiral, potentially porous materials through spontaneous resolution of conformers of a PCP pincer palladium complex ({2,6-bis[(di-t-butylphosphino)methyl]phenyl}palladium(II)halide). The crystallisation is controlled by weak hydrogen bonding giving rise to chiral qtz-nets and channel structures, as shown by 16 such crystal structures for X = Cl and Br with various solvents like pentane and bromobutane.

The formation of CuCl2-specific metallogels of pyridyloxalamide derivatives in alcohols.

Isomeric pyridyloxalamide derivatives 1-3, which differed in the position of the nitrogen atom on the pyridyl ring, showed remarkably different gel-forming aptitudes in the presence of CuCl2 salt in alcohols. Whilst derivatives 1 and 3 formed a soluble complex and a solid precipitate, respectively, ligand 2 generated a remarkably metal- and anion-specific metallogel.

Neutral Organometallic Halogen Bond Acceptors: Halogen Bonding in Complexes of PCPPdX (X = Cl, Br, I) with Iodine (I(2)), 1,4-Diiodotetrafluorobenzene (F4DIBz), and 1,4-Diiodooctafluorobutane (F8DIBu).

The behavior of a sterically crowded neutral pincer {2,6-bis[(di-t-butylphosphino)methyl]-phenyl}palladium (PCPPd) halides, PCPPdX (X = Cl, Br or I), as XB acceptors with strong halogen bond (XB) donors, iodine (I(2)), 1,4-diiodotetrafluorobenzene (F4DIBz), and 1,4-diiodooctafluorobutane (F8DIBu) were studied in the solid state. The co-crystallization experiments afforded high-quality single crystals of XB complexes PCPPdCl-I(2) (1a), PCPPdBr-I(2) (2a), PCPPdI-I(2)(3a), PCPPdCl-F4DIBz (1b), PCPPdBr-F4DIBz (2b), and PCPPdBr-F8DIBu (2c). The 1:1 iodine complexes (1a, 2a, and 3a) all showed a strong halogen bonding interaction, the reduction of the sum of the van der Waals radii of halogen to iodine being 24.

Fluoride-responsive organogelator based on oxalamide-derived anthraquinone.

Anthraquinone derived oxalamide gelator 1 forms with aromatic solvents and alcohols very stable gels which selectively respond to the presence of fluoride anion by colour change and/or gel-to-sol transition.

Synthesis, structural studies, and biological evaluation of some purine substituted 1-aminocyclopropane-1-carboxylic acids and 1-amino-1-hydroxymethylcyclopropanes.

The novel purine derivatives of 1-aminocyclopropane-1-carboxylic acid (8 and 9) and 1-amino-1-hydroxymethylcyclopropane (12 and 13) with methylene spacer between the base and the cyclopropane ring were prepared by multistep synthetic route involving alkylation of adenine and 6-(N-pyrrolyl)purine with 2-hydroxy-methyl-1-aminocyclopropane-1-carboxylic acid derivative 3 as a key reaction. All novel compounds were racemic. The N-9 substitution of the purine ring and the Z-configuration of the cyclopropane ring in 4-13 were deduced from their 1H and 13C NMR spectra by analyses of chemical shifts, H-H coupling constants and connectivities in two-dimensional homo- and heteronuclear correlation spectra.

Hydrogen bonding in N,N'-bis[(1S)-2-azido-1-(2-methylpropyl)ethyl]oxalamide: twofold symmetry of R(2)(2)(10) hydrogen-bonded dimers connected into an alpha-network.

The title compound, C(14)H(26)N(8)O(2), belongs to a class of retropeptides with an oxalamide unit (-NH-CO-CO-NH-), and is a precursor for the synthesis of an amine-terminal gelator. The compound is a good synthon for one-dimensional hydrogen bonding. The crystal structure reveals a hydrogen-bonded cyclic dimer with unusual twofold rotation symmetry.